The most common Robertsonian translocation in humans is a 13/14 fusion chromosome. The cytogenetic designation of a balanced carrier is either 45,XY,rob(13;14) (q10;q10) or 45,XY,der(13;14) (q10;q10). This nomenclature means that there are 45 chromosomes in the cells with a normal male sex chromosome complement and a Robertsonian translocation.. Introduction. Robertsonian (rob) translocation is the most common form of structural chromosomal abnormality or rearrangement [1-3].One in 1,000 healthy individuals is thought to carry a Robertsonian translocation inherited from one of the parents with a normal phenotype [2-4].A Robertsonian translocation involves only the acrocentric chromosomes (13, 14, 15, 21, and 22).
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Robertsonian Translocation 13 14
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question about robertsonian translocation r/Mcat
Robertsonian translocation ( ROB) is a chromosomal abnormality where the entire long arms of two different chromosomes become fused to each other. It is the most common form of chromosomal translocation in humans, affecting 1 out of every 1,000 babies born. [1] It does not usually cause medical problems, though some people may produce gametes.. La traslocazione robertsoniana t (13;14) (q10;q10), è bilanciata e determinata tra il braccio lungo di un cromosoma 13 ed il braccio lungo di un cromosoma 14. I problemi di chi porta tale traslocazione sono essenzialmente legati alla funzione riproduttiva, in quanto essi risultano a rischio di produrre gameti sbilanciati.
